This study is exploring a new once-a-week treatment for HIV-1, combining Islatravir (ISL) and Ulonivirine (ULO). Researchers want to see if this treatment is as effective as the daily pill, BIC/FTC/TAF. They will check this by measuring how many people still have a high virus level in their blood after 24 weeks. They will also assess the safety of the new treatment and how well people tolerate it.
- Study Duration: 24 weeks
- Eligibility: Participants must have been on the current treatment BIC/FTC/TAF with good virus control for at least 6 months.
- Exclusions: People with HIV-2, active AIDS-related infections, hepatitis C or B, certain recent cancers, or previous use of ISL/ULO cannot join.
Participants should understand the study involves trying a new treatment, which may carry unknown risks. Before joining, they should consider the benefits of a weekly dose compared to the daily routine, and the commitment to attend study visits. Always consult your healthcare provider before enrolling in a clinical study.